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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500525Generated: November 1, 2026

4-Bromophenacyl bromide → HCID 56962039, compound

https://huagongshe.com/reaction/1500525

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromophenacyl bromideHCID 7454—
ReactantDiisopropylethylamineHCID 81531—
ReactantAmmonium AcetateHCID 517165—
Reactant(4S)-1-(tert-Butoxycarbonyl)-4-methoxy-L-prolineHCID 15222286—
SolventDichloromethaneHCID 6344—
ProductHCID 56962039HCID 5696203996.1%

Reaction Conditions

Temperature35 °C

Reaction Steps

To a solution of (2S,4S)-4-methoxy-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester (900 mg, 3.67 mmol), and p-bromophenacyl bromide (1.02 g, 3.67 mmol) in DCM (20 mL) under nitrogen, was added N,N-diisopropylethylamine (1.92 mL, 11.01 mmol). The resulting mixture was stirred at 35° C. for 3 h and concentrated under vacuum. The crude intermediate was dissolved in toluene (150 mL), ammonium acetate (5.66 g, 73.4 mmol) was added, and the resulting mixture was stirred at 95° C. overnight, cooled to RT, and washed with water (2×10 mL). The organic layer was dried over magnesium sulfate, filtered, concentrated and purified by silica gel chromatography (24 g, ethyl acetate/hexanes 0 to 60%) to give the title intermediate (1.49 g, 96% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206159B2
Source datasetuspto-grants-2015_12
ORD IDord-39f2ffc450a34c12b083a48bf925c29c
Source noteuspto-grants-2015_12